FDAFDA · Food and drugs·Recall number D-0438-2017
DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56
Published February 1, 2017 · Recall initiated: January 16, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/ Degradation Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
- Distributor
- Nationwide
- Lot
- Lot # 0000007104; Exp 05/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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